A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3978645



Internal ID18892072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:77977016..78776824hg38UCSC Ensembl
Outerchr15:78269358..79069166hg19UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg38799809
hg19799809
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1116464
Supporting Variants
SamplesKWS2
Known GenesACSBG1, ADAMTS7, CHRNA3, CHRNA5, CHRNB4, CIB2, CRABP1, DNAJA4, HYKK, IDH3A, IREB2, LOC646938, LOC91450, MIR5003, PSMA4, SH2D7, TBC1D2B, WDR61
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3978645
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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